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A Virginia woman recently filed a Xarelto law suit claiming that her husband suffered serious injuries that led to his death as a result of use of Xarelto.
The plaintiff seeks $2 million in damages.
Xarelto Side Effects are very serious and have been previously linked to at least 370 deaths, according to a Chicago Tribune report.
More than 18,000 Xarelto lawsuits have been centralized in federal multidistrict litigation (MDL) in U.S. District Court, Eastern District of Louisiana, where Judge Eldon Fallon has selected four bellwether cases to be tried in Louisiana, Mississippi, and Texas during the coming year.
In the first trial, a jury found that the companies were not responsible for a Xarelto user’s internal bleeding, but the companies face three more Xarelto trials in the next few months.
Xarelto is a blood thinner prescribed to patients suffering from atrial fibrillation (irregular heart beat) who are at increased risk of formed a blood clot in the heart, which can travel to the brain and cause a stroke.
Xarelto was jointly developed by Bayer and Johnson & Johnson.
Xarelto was Bayer’s top selling drug in 2016, earning more than $3 billion in sales and earning more than $2.2 billion for J&J that same year.
Although all blood thinners increase the risk of bleeding problems, Xarelto has been linked to an increased number of uncontrollable bleed injuries, mostly because there is no approved antidote available for patients who use the medication, and many of the side effects have been severe because the bleeding cannot be effectively controlled.
Since approval in 2011, Xarelto has been the subject of two black box warnings issued by the FDA.
In August 2013, Xarelto received a black box warning indicating that the premature discontinuation of Xarelto increases the risk of thrombotic events and spinal/epidural hematoma in patients.
Then in March 2014, Xarelto received another black box warning cautioning that the ideal timing between the administration of Xarelto and neuraxial procedures in each individual patient is not known.
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With over 25 years of legal experience, Jessie is an Illinois lawyer, a CPA, and a mother of three. She spent the first decade of her career working as an international tax attorney at Deloitte.
In 2009, Jessie co-founded her own law firm with her husband – which has scaled to over 30 employees since its conception.
In 2016, Jessie founded TruLaw, which allows her to collaborate with attorneys and legal experts across the United States on a daily basis. This hypervaluable network of experts is what enables her to share reliable legal information with her readers!
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AFFF Lawsuit claims are being filed against manufacturers of aqueous film-forming foam (AFFF), commonly used in firefighting.
Claims allege that companies such as 3M, DuPont, and Tyco Fire Products failed to adequately warn users about the potential dangers of AFFF exposure — including increased risks of various cancers and diseases.
Suboxone Tooth Decay Lawsuit claims are being filed against Indivior, the manufacturer of Suboxone, a medication used to treat opioid addiction.
Claims allege that Indivior failed to adequately warn users about the potential dangers of severe tooth decay and dental injuries associated with Suboxone’s sublingual film version.
Social Media Harm Lawsuits are being filed against social media companies for allegedly causing mental health issues in children and teens.
Claims allege that companies like Meta, Google, ByteDance, and Snap designed addictive platforms that led to anxiety, depression, and other mental health issues without adequately warning users or parents.
Transvaginal Mesh Lawsuits are being filed against manufacturers of transvaginal mesh products used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI).
Claims allege that companies like Ethicon, C.R. Bard, and Boston Scientific failed to adequately warn about potential dangers — including erosion, pain, and infection.
Bair Hugger Warming Blanket Lawsuits involve claims against 3M — alleging their surgical warming blankets caused severe infections and complications (particularly in hip and knee replacement surgeries).
Plaintiffs claim 3M failed to warn about potential risks — despite knowing about increased risk of deep joint infections since 2011.
Baby Formula NEC Lawsuit claims are being filed against manufacturers of cow’s milk-based baby formula products.
Claims allege that companies like Abbott Laboratories (Similac) and Mead Johnson & Company (Enfamil) failed to warn about the increased risk of necrotizing enterocolitis (NEC) in premature infants.
Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?